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  1. CFR 1020.32 Fluoroscopic equipment (a) Primary protective barrier
  2. CFR 1020.32 Fluoroscopic equipment (b)(1) Angulation
  3. CFR 1020.32 Fluoroscopic equipment (b)(2) Further means for limitation
  4. CFR 1020.32 Fluoroscopic equipment (b)(3) Non-image-intensified fluoroscopy
  5. CFR 1020.32 Fluoroscopic equipment (b)(4) Circular image receptors
  6. CFR 1020.32 Fluoroscopic equipment (b)(5) Rectangular image receptors
  7. CFR 1020.32 Fluoroscopic equipment (b)(6) Override capability
  8. CFR 1020.32 Fluoroscopic equipment (c) Activation of tube
  9. CFR 1020.32 Fluoroscopic equipment (d)(1) equipment manufactured before May 19, 1995
  10. CFR 1020.32 Fluoroscopic equipment (d)(2) Optional clause for high-level control
  11. CFR 1020.32 Fluoroscopic equipment (d)(2) equipment manufactured on or after May 19, 1995
  12. CFR 1020.32 Fluoroscopic equipment (d)(3) Measuring compliance
  13. CFR 1020.32 Fluoroscopic equipment (d)(4) Exemptions
  14. CFR 1020.32 Fluoroscopic equipment (f) Indication of potential and current
  15. CFR 1020.32 Fluoroscopic equipment (g) Source-skin distance
  16. CFR 1020.32 Fluoroscopic equipment (h)(1) Fluoroscopic irradiation time, display, and signal before June 10 2006
  17. CFR 1020.32 Fluoroscopic equipment (h)(2) Fluoroscopic irradiation time, display, and signal after June 10 2006
  18. CFR 1020.32 Fluoroscopic equipment (j) Display of last-image-hold (LIH)
  19. CFR 1020.32 Fluoroscopic equipment (k) Displays of values of AKR and cumulative air kerma
  20. CFR 21-007 - Enforcement Policy - Recalls
  21. CFR 21-011 - Electronic Records; Electronic Signatures
  22. CFR 21-1010 - Performance Standards for Electronics Products
  23. CFR 21-801 - Labeling
  24. CFR 21-803 - Medical Device Reporting
  25. CFR 21-806 - Medical Devices; reports of corrections and removals
  26. CFR 21-807 - Establishment Registration and Device Listing
  27. CFR 21-814 - Premarket Approval of Medical Devices
  28. CFR 21-820.20 - Management Control Flowchart
  29. CFR 21-820.20 - Management Responsibility
  30. CFR 21-820.20a - Quality System
  31. CFR 21-820.20b - Organization
  32. CFR 21-820.20c - Management review
  33. CFR 21-820.20d - Quality Planning
  34. CFR 21-820.20e - Quality System Procedures
  35. CFR 21-820.25 - Personnel
  36. CFR 21-820.25 - Personnel - General
  37. CFR 21-820.25 - Personnel - Training
  38. CFR 21-820.30 - Design Controls
  39. CFR 21-820.30 - FDA Inspection Guidelines
  40. CFR 21-820.30a - General
  41. CFR 21-820.30b - Design and development planning
  42. CFR 21-820.30c - Design Input
  43. CFR 21-820.30d - Design Output
  44. CFR 21-820.30e - Design Review
  45. CFR 21-820.30f - Design Verification
  46. CFR 21-820.30g - Design Validation
  47. CFR 21-820.30h - Design Transfer
  48. CFR 21-820.30i - Design Changes
  49. CFR 21-820.30j - Design History File
  50. CFR 21-820.40a - Document approval and distribution

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